Model MS-2 Handpiece

FDA 510(k) K982050 · Parkell, Inc.

Substantially Equivalent

510(k) numberK982050

Submission

Device name
Model MS-2 Handpiece
Applicant
Parkell, Inc.
Farmingdale, NY, US
Received
June 11, 1998
Decision date
September 2, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EFB – Handpiece, Air-Powered, Dental
Device class
Class I (low risk)
Regulation
21 CFR 872.4200
Specialty
Dental

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Questions and answers

When was Model MS-2 Handpiece cleared by the FDA?

Model MS-2 Handpiece (K982050) received a 510(k) decision of Substantially Equivalent on September 2, 1998, 83 days after the submission was received.

What is the product code of K982050?

The FDA product code is EFB – Handpiece, Air-Powered, Dental, a Class I (low risk) device regulated under 21 CFR 872.4200.